All diseases

3 entries on 1 page. Showing entries 1 - 3.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00387 ESCS S-cone syndrome, enhanced (ESCS, Goldmann-Favre syndrome) 268100 - 70 70 NR2E3 - -
00112 RP retinitis pigmentosa (RP) 268000 - 160 115 ARL3, BEST1, DHDDS, NR2E3, SLC7A14 - -
00386 RP37 retinitis pigmentosa, type 37 (RP37) 611131 - 0 0 NR2E3 - -
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